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CAS 76265-70-8

:

(2S)-2-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]-4-(methylsulfinyl)butanoic acid

Description:
The chemical substance known as (2S)-2-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]-4-(methylsulfinyl)butanoic acid, with the CAS number 76265-70-8, is a derivative of an amino acid featuring a fluorenylmethoxycarbonyl (Fmoc) protecting group. This compound is characterized by its chiral center at the second carbon, which contributes to its stereochemistry and biological activity. The presence of the methylsulfinyl group indicates that it contains a sulfur atom, which can influence its reactivity and solubility. The Fmoc group is commonly used in peptide synthesis as a protective group for the amino functionality, allowing for selective reactions. This compound is likely to be soluble in organic solvents and may exhibit specific interactions with biological targets due to its structural features. Additionally, its application in peptide synthesis and potential use in pharmaceuticals highlight its significance in organic and medicinal chemistry. Overall, this compound exemplifies the complexity and functionality of modified amino acids in chemical research and development.
Formula:C20H21NO5S
InChI:InChI=1S/C20H21NO5S/c1-27(25)11-10-18(19(22)23)21-20(24)26-12-17-15-8-4-2-6-13(15)14-7-3-5-9-16(14)17/h2-9,17-18H,10-12H2,1H3,(H,21,24)(H,22,23)/t18-,27?/m0/s1
InChI key:InChIKey=CEHRSUBRZOGRSW-HSYKDVHTSA-N
SMILES:C(OC(N[C@@H](CCS(C)=O)C(O)=O)=O)C1C=2C(C=3C1=CC=CC3)=CC=CC2
Synonyms:
  • (2S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-(methylsulfinyl)butanoic acid
  • (2S)-2-([[(9H-Fluoren-9-yl)methoxy]carbonyl]amino)-4-methanesulfinylbutanoic acid
  • (2S)-2-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]-4-(methylsulfinyl)butanoic acid
  • Butanoic acid, 2-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-4-(methylsulfinyl)-, (2S)-
  • Fmoc-L-methionine-sulfoxide
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